FREE ON-DEMAND WEBINAR
As events surrounding the coronavirus (COVID-19) continue to unfold, medical device companies are finding themselves facing unforeseen challenges, whether that be centralized teams now being forced to collaborate and access information remotely, clinical trials being delayed, or a myriad of other issues caused by the "new normal".
Based on data-driven insights from medical device industry professionals in the 2020 State of Medical Device Product Development & Quality Management Report, we know medical device companies’ ability to collaborate will be disrupted based on the fact that:
And yet companies that indicated that they were using best-in-class software for managing product development and quality activities are:
This in-depth webinar will cover how companies using turn-key, best-in-class QMS software are able to remain agile in order to innovate and outperform the competition.
Greenlight Guru is the only quality management software platform designed specifically for medical device companies. The platform helps companies bring safer products to market faster, simplifies FDA and ISO regulatory compliance and provides a single source of truth by connecting the management of all quality processes like CAPAs, risk, audits and more. Greenlight Guru’s platform is used by thousands of users across the globe to push beyond baseline compliance and achieve True Quality for their medical devices.